A convenient synthesis of 1‐methyl‐4‐oxopiṕecolic acid methyl ester

M. Y. Essawi; P. S. Portoghese

doi:10.1002/jhet.5570200245

A convenient synthesis of 1‐methyl‐4‐oxopiṕecolic acid methyl ester

M. Y. Essawi, P. S. Portoghese

Medicinal Chemistry

Research output: Contribution to journal › Comment/debate › peer-review

6 Scopus citations

Abstract

An efficient and convenient synthesis of the title compond 1 is described. The approach to the synthesis is based on hydride reduction of the 4‐methoxypyridinium salt 5, followed by acid hydrolysis of the resulting vinyl ether intermediate 6.

Original language	English (US)
Pages (from-to)	477-478
Number of pages	2
Journal	Journal of Heterocyclic Chemistry
Volume	20
Issue number	2
DOIs	https://doi.org/10.1002/jhet.5570200245
State	Published - Jan 1 1983

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title = "A convenient synthesis of 1‐methyl‐4‐oxopiṕecolic acid methyl ester",

abstract = "An efficient and convenient synthesis of the title compond 1 is described. The approach to the synthesis is based on hydride reduction of the 4‐methoxypyridinium salt 5, followed by acid hydrolysis of the resulting vinyl ether intermediate 6.",

author = "Essawi, \{M. Y.\} and Portoghese, \{P. S.\}",

year = "1983",

month = jan,

day = "1",

doi = "10.1002/jhet.5570200245",

language = "English (US)",

volume = "20",

pages = "477--478",

journal = "Journal of Heterocyclic Chemistry",

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TY - JOUR

T1 - A convenient synthesis of 1‐methyl‐4‐oxopiṕecolic acid methyl ester

AU - Essawi, M. Y.

AU - Portoghese, P. S.

PY - 1983/1/1

Y1 - 1983/1/1

N2 - An efficient and convenient synthesis of the title compond 1 is described. The approach to the synthesis is based on hydride reduction of the 4‐methoxypyridinium salt 5, followed by acid hydrolysis of the resulting vinyl ether intermediate 6.

AB - An efficient and convenient synthesis of the title compond 1 is described. The approach to the synthesis is based on hydride reduction of the 4‐methoxypyridinium salt 5, followed by acid hydrolysis of the resulting vinyl ether intermediate 6.

UR - https://www.scopus.com/pages/publications/84986495502

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U2 - 10.1002/jhet.5570200245

DO - 10.1002/jhet.5570200245

M3 - Comment/debate

AN - SCOPUS:84986495502

SN - 0022-152X

VL - 20

SP - 477

EP - 478

JO - Journal of Heterocyclic Chemistry

JF - Journal of Heterocyclic Chemistry

IS - 2

ER -

A convenient synthesis of 1‐methyl‐4‐oxopiṕecolic acid methyl ester

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